# FDA recall Z-0337-2020

> **Zimmer Biomet, Inc.** · Class II · device recall initiated 2019-10-10.

## Product

Cephalomedullary Nail (CMN), Various sizes, Item Nos. 47249318009  47249318010  47249318011  47249318013  47249318014  47249318109  47249318110  47249318111  47249318113  47249318114  47249318209  47249318210  47249318211  47249318213  47249318214  47249318309  47249318310  47249318311  47249318313  47249318314  47249321010  47249321011  47249321013  47249321014  47249321110  47249321111  47249321113  47249321114  47249321210  47249321211  47249321213  47249321214  47249321310  47249321311  47249321313  47249321314  47249321410  47249321411  47249321413  47249321414  47249321510  47249321511  47249321513  47249321514  47249330010  47249330011  47249330013  47249330110  47249330111  47249330113  47249330210  47249330211  47249330213  47249330310  47249330311  47249330313  47249330410  47249330411  47249330413  47249330510  47249330511  47249330513  47249332010  47249332011  47249332013  47249332110  47249332111  47249332113  47249332210  47249332211  47249332213  47249332310  4724933231

## Reason for recall

Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).

## Distribution

Distributed nationwide.

## Key facts

- **Recall number:** Z-0337-2020
- **Recalling firm:** Zimmer Biomet, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-10-10
- **Report date:** 2019-11-13
- **Termination date:** 2020-05-19

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Warsaw, IN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0337-2020

## Citation

> AI Analytics. FDA recall Z-0337-2020. Retrieved 2026-06-08 from https://api.ai-analytics.org/recall/Z-0337-2020. Source: US FDA. Licensed CC0.

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